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21.
Boon-Seang Chu Sosaku Ichikawa Sumiyo Kanafusa Mitsutoshi Nakajima 《Journal of the American Oil Chemists' Society》2007,84(11):1053-1062
This work was initiated to prepare protein-stabilized β-carotene nanodispersions using emulsification–evaporation. A pre-mix
of the aqueous phase composed of a protein and hexane containing β-carotene was subjected to high-pressure homogenization
using a microfluidizer. Hexane in the resulting emulsion was evaporated under reduced pressures, causing crystallization and
precipitation of β-carotene inside the droplets and formation of β-carotene nanoparticles. Sodium caseinate (SC) was the most
effective emulsifier among selected proteins in preparing the nanodispersion, with a monomodal β-carotene particle-size distribution
and a 17-nm mean particle size. The results were confirmed by transmission-electron microscopy analysis. SC-stabilized nanodispersion
also had considerably high ζ-potential (−27 mV at pH 7), suggesting that the nanodispersion was stable against particle aggregation.
Increasing the SC concentration decreased the mean particle size and improved the polydispersity of the nanodispersions. Nanodispersions
prepared with higher β-carotene concentrations and higher organic-phase ratios resulted in larger β-carotene particles. Although
increased microfluidization pressure did not decrease particle size, it did improve the polydispersity of the nanodispersions.
Repeating the microfluidization process at 140 MPa caused the nanodispersions to become polydisperse, indicating the loss
of emulsifying capacity of SC due to protein denaturation. 相似文献
22.
The objective of this study was to examine how and to what extent a new degradable polymeric fiber, poly(p-dioxanone), used as a surgical suture material, degrades in the presence of enzymes and after γ-irradiation. The degradation of the fiber was studied mechanically using an Instron and morphologically by SEM. Both esterase and trypsin enzymes and their corresponding buffer controls were used. The fibers were γ-irradiated at the dosages ranging from 0 to 20 Mrad, immersed in the solution for up to 70 days, and then removed for tensile strength and morphological examinations. It was found that γ-irradiation alone lowered the tensile strength of PDS fibers and made them more susceptible to hydrolysis. Esterase and trypsin did not accelerate the hydrolytic degradtion of this fiber to any significant level. Both γ-irradiation and enzymes influenced the gross morphological characteristic of PDS fibers when they were subjected to hydrolysis. The most important morphological observations were the formation of surface cracks and chips on the fibers and the subsequent peeling of the chips. Enzyme-treated PDS fibers exhibited similar morphological findings but the size of the chips was smaller. The morphological observations of PDS fibers were consistent with the tensile strength data. 相似文献
23.
C. C. Chu 《应用聚合物科学杂志》1981,26(5):1727-1734
The hydrolytic degradation of polyglycolic acid (PGA) was studied by examining the changes of tensile strength and the level of crystallinity of the suture material. It was found that the breaking stress decreased from 6.369 × 10?1 at 0 day to 3.97 × 10?3 Newton/Tex at 49 days. The sigmodial shape of the stress–strain curves gradually disappeared with increase in the duration of in vitra degradation. The endpoint titration method used to assess the degree of degradation beyond the period of measurable tensile strength showed that the percent of PGA degraded were 42, 56, and 70% at 49, 60, and 90 days, respectively. The level of crystallinity of PGA at various durations of degradation exhibited an initial increase in the degree of crystallinity from 40% at 0 day to an upper limit of 52% at 21 days, then gradual decrease to 23% at 90 days. This observation is essentially parallel to hydrolysis of cellulose and polyethylene terephthalate. The concept of microfibrillar structure of fibers provides the basis for the proposed degradation mechanism of PGA in vitro. It is believed that degradation proceeds through two main stages which are different in rate of degradation. 相似文献
24.
We have examined the rheological properties of a Co-adsorbed γ-Fe2O3 magnetic suspension with polyurethane (PU) as a binder and methyl ethyl ketone (MEK) or cyclohexanone (CH) as a solvent. A Haake RV20 viscometer was used to measure the suspension viscosity and the vane method was adopted to determine the fluid yield stress. A rheological model which can be viewed as a combination of the Casson model and the Bingham model is proposed to describe the suspension viscosity. The effects of temperature, particle content, and binder concentration are included in the model. 相似文献
25.
A study has been made of the cathodic deposition of copper ions from flowing dilute aqueous solutions onto a packed bed of graphite. The electrodeposition reaction is mass transfer controlled and expressions are presented for the cathodic current as a function of time, solution flow rate and bed characteristics. These have been verified from potentiostatic experiments. The cathode current efficiency is shown to approach 100% and packed bed electrodes are shown to be an effective means of extracting or removing metal ions from dilute solutions. 相似文献
26.
The activities of several commercial nickel catalysts were determined by measuring their activation energies. Among these
catalysts, G95E, Resan 22, Nysosel 222 and 325, all with low activation energy, were more active than DM3 and G95H, which
had higher activation energy. However, the less active catalysts increased the linoleate selectivity of soybean oil during
hydrogenation. The yields of bothtrans isomers and winterized oil were higher for the more selectively hydrogenated oil catalyzed by the less active catalysts.
In the sensory evaluation, the fractionated solid fat that contained moretrans isomers was lower in flavor scores than the fractionated liquid oil after hydrogenation and winterization of soybean oil. 相似文献
27.
28.
This paper presents a mathematical model based on the reaction rate expressions to describe the displacement of methane conversion in the steam reforming. The effect of several parameters including weight hourly space velocity (WHSV), load-to-surface ratio, reaction pressure, hydrogen partial pressure in permeate side and reaction temperature were investigated. Simulation and experimental results showed that a conversion higher than 80% could be achieved in a palladium membrane reactor at reaction temperature of 500 °C relative to 850 °C in a conventional fixed bed reactor (FBR). Besides, the yield of CO (<2%) in membrane reactor was much lower than that (>50%) in the FBR, which indicated the significant depression of CO production in use of membrane reactor. 相似文献
29.
A mathematical model of fluid flow and mass transfer in a packed bed was derived and used to evaluate the liquid phase axial dispersion and mass transfer coefficients under high pressure conditions. The least-squares method was used to evaluate the rate parameters from experimental breakthrough curves, and the agreement between the concentration curves predicted from rate parameters and those measured experimentally was good. Experiments were performed at 20 and 200°C with water as a solvent and nonporous soda-lime glass beads as packing. Although the axial dispersion coefficient was independent of temperature and pressure, the mass transport parameters were found to be pressure dependent. 相似文献
30.
The viscoelastic properties of a rubber–resin blend, which influences performance of the blend as a pressure-sensitive adhesive, depend upon the structure of the resin as well as its molecular weight. The effect of the concentration of a compatible resin in the blend was examined using a mechanical spectrometer. Four types of resins were used. These are the rosin esters, polyterpenes, pure monomer resins such as polystyrene and poly(vinyl cyclohexane), and petroleum stream resins. Each was examined in blends with both natural rubber and styrene–butadiene rubber over a range of concentrations. It is shown that the temperature of the tan δ peak for compatible systems can be predicted by the Fox equation, T = W1T + W2T, where W1 and W2 are the weight fractions of the resin and rubber, respectively, and the Tg's are the tan δ peak temperatures in K. The plateau modulus G for a blend can be identified as the G′ value in the rubbery plateau at the point where tan δ is at a minimum. The relationship between G and G, the plateau modulus for the undiluted elastomer, is shown to be proportional to the volume fraction of the elastomer raised to the 2.3–2.4 power for natural rubber with six different compatible resins. The exponent for styrene–butadiene rubber is 2.5–2.6 with four different resins. Using these relationships, both the tan δ peak temperature and plateau modulus can be predicted for a rubber–resin system from data on the unmodified elastomer and on one typical rubber–resin blend. 相似文献